Data / Medical devices / United States / Medrange Corporation

Medrange Corporation: FDA-registered device maker in Brea, CA, United States, 6 510(k) clearances

Name: Medrange Corporation FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Medrange Corporation is registered with the FDA (registration 3008786200) in Brea, CA, United States. It lists 3 device types. The FDA files 6 510(k) clearances under its listings, the newest dated April 10, 2026. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Get makers like this one Watch Medrange Corporation

FDA registration number: 3008786200
Address: 480 Apollo St Ste D, Brea, CA, United States, 92821
Owner or operator: Medrange Corporation (10034563)
Roles: Manufacturer, Specification developer
First device listed: December 13, 2010
Registered through: 2026
Brand names listed: 8070 Accsurg Electrosurgical Workstation and Accessories, 8Q10 Surclear Smoke Plume Evacuation System, EES 100 Electrosurgical Expansion System with Accessories, MB8010 Electrosurgical Generator, Medrange MB 8010 Electrosurcical Generator, Surn5 Electrosurgical Argon Beam Generator and Accessories, T61 Surgical Table

Devices it lists

Device	Product code	Class	Role	Source
Apparatus, Exhaust, Surgical	FYD	2	Specification developer	accessdata.fda.gov
Electrosurgical, Cutting & Coagulation & Accessories	GEI	2	Manufacturer, Specification developer	accessdata.fda.gov
Table, Operating-Room, Ac-Powered	FQO	1	Specification developer	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
April 10, 2026	K253777	Ascblue (8010)	GEI	Substantially Equivalent	Ascblue Corporation	accessdata.fda.gov
April 10, 2024	K233789	8Q10 Surclear Smoke Plume Evacuation System	FYD	Substantially Equivalent	Surnic Corporation	accessdata.fda.gov
February 22, 2021	K203522	Surn5 Electrosurgical Argon Beam Generator and Accessories	GEI	Substantially Equivalent	Surnic Corporation	accessdata.fda.gov
September 18, 2020	K201224	Electrosurgical Generator and Accessories	GEI	Substantially Equivalent	Medrange	accessdata.fda.gov
October 23, 2012	K122092	MEDRANGE ELECTROSURGICAL EXPANSION SYSTEM	GEI	Substantially Equivalent	Medrange Corporation	accessdata.fda.gov
November 22, 2010	K102114	MEDRANGE ELECTROSURGICAL GENERATOR	GEI	Substantially Equivalent	Medrange Corporation	accessdata.fda.gov

Compare with other makers

Updated April 10, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.